PPS, a Large Multidomain Protein, Functions with Sex-Lethal to Regulate Alternative Splicing in
Alternative splicing controls the expression of many genes, including the Drosophila sex determination gene Sex-lethal (Sxl). Sxl expression is controlled via a negative regulatory mechanism where inclusion of the translation-terminating male exon is blocked in females. Previous studies have shown that the mechanism leading to exon skipping is autoregulatory and requires the SXL protein to antagonize exon inclusion by interacting with core spliceosomal proteins, including the U1 snRNP protein Sans-fille (SNF). In studies begun by screening for proteins that interact with SNF, we identified PPS, a previously uncharacterized protein, as a novel component of the machinery required for Sxl male exon skipping. PPS encodes a large protein with four signature motifs, PHD, BRK, TFS2M, and SPOC, typically found in proteins involved in transcription. We demonstrate that PPS has a direct role in Sxl male exon skipping by showing first that loss of function mutations have phenotypes indicative of Sxl misregulation and second that the PPS protein forms a complex with SXL and the unspliced Sxl RNA. In addition, we mapped the recruitment of PPS, SXL, and SNF along the Sxl gene using chromatin immunoprecipitation (ChIP), which revealed that, like many other splicing factors, these proteins bind their RNA targets while in close proximity to the DNA. Interestingly, while SNF and SXL are specifically recruited to their predicted binding sites, PPS has a distinct pattern of accumulation along the Sxl gene, associating with a region that includes, but is not limited to, the SxlPm promoter. Together, these data indicate that PPS is different from other splicing factors involved in male-exon skipping and suggest, for the first time, a functional link between transcription and SXL–mediated alternative splicing. Loss of zygotic PPS function, however, is lethal to both sexes, indicating that its role may be of broad significance.
Vyšlo v časopise:
PPS, a Large Multidomain Protein, Functions with Sex-Lethal to Regulate Alternative Splicing in. PLoS Genet 6(3): e32767. doi:10.1371/journal.pgen.1000872
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1000872
Souhrn
Alternative splicing controls the expression of many genes, including the Drosophila sex determination gene Sex-lethal (Sxl). Sxl expression is controlled via a negative regulatory mechanism where inclusion of the translation-terminating male exon is blocked in females. Previous studies have shown that the mechanism leading to exon skipping is autoregulatory and requires the SXL protein to antagonize exon inclusion by interacting with core spliceosomal proteins, including the U1 snRNP protein Sans-fille (SNF). In studies begun by screening for proteins that interact with SNF, we identified PPS, a previously uncharacterized protein, as a novel component of the machinery required for Sxl male exon skipping. PPS encodes a large protein with four signature motifs, PHD, BRK, TFS2M, and SPOC, typically found in proteins involved in transcription. We demonstrate that PPS has a direct role in Sxl male exon skipping by showing first that loss of function mutations have phenotypes indicative of Sxl misregulation and second that the PPS protein forms a complex with SXL and the unspliced Sxl RNA. In addition, we mapped the recruitment of PPS, SXL, and SNF along the Sxl gene using chromatin immunoprecipitation (ChIP), which revealed that, like many other splicing factors, these proteins bind their RNA targets while in close proximity to the DNA. Interestingly, while SNF and SXL are specifically recruited to their predicted binding sites, PPS has a distinct pattern of accumulation along the Sxl gene, associating with a region that includes, but is not limited to, the SxlPm promoter. Together, these data indicate that PPS is different from other splicing factors involved in male-exon skipping and suggest, for the first time, a functional link between transcription and SXL–mediated alternative splicing. Loss of zygotic PPS function, however, is lethal to both sexes, indicating that its role may be of broad significance.
Zdroje
1. SalzHK
Erickson
JW
2010 Sex determination in Drosophila: the view from the top. Fly In Press
2. NagengastAA
StitzingerSM
TsengC-H
MountSM
SalzHK
2003 Sex-lethal splicing autoregulation in vivo: interactions between SEX-LETHAL, the U1 snRNP and U2AF underlie male exon skipping. Development 130 463 471
3. PennJK
GrahamP
DeshpandeG
CalhounG
ChaoukiAS
2008 Functioning of the Drosophila Wilms'-tumor-1-associated protein homolog, Fl(2)d, in Sex-lethal-dependent alternative splicing. Genetics 178 737 748
4. ChaoukiAS
SalzHK
2006 Drosophila SPF45: a bi-functional protein with roles in both splicing and DNA repair. PLoS Genet 2 e178 doi:10.1371/journal.pgen.0020178
5. SalzHK
2007 Male or female? The answer depends on when you ask. PLoS Biol 5 e335 doi:10.1371/journal.pbio.0050335
6. EricksonJW
QuinteroJJ
2007 Indirect effects of ploidy suggest X chromosome dose, not the X:A ratio, signals sex in Drosophila. PLoS Biol 5 e332 doi:10.1371/journal.pbio.0050332
7. GonzalezAN
LuH
EricksonJW
2008 A shared enhancer controls a temporal switch between promoters during Drosophila primary sex determination. Proc Natl Acad Sci U S A 105 18436 18441
8. ParksAL
CookKR
BelvinM
DompeN
FawcettR
2004 Systematic generation of high-resolution deletion coverage of the Drosophila melanogaster genome. Nat Gen 36 288 292
9. RyderE
BlowsF
AshburnerM
Bautista-LlacerR
CoulsonD
2004 The DrosDel collection: a set of P-element insertions for generating custom chromosomal aberrations in Drosophila melanogaster. Genetics 167 797 813
10. ChauJ
KulnaneLS
SalzHK
2009 Sex-lethal facilitates the transition from germline stem cell to committed daughter cell in the Drosophila ovary. Genetics 182 121 132
11. CronmillerC
ClineTW
1986 The relationship of relative gene dose to the complex phenotype of the daughterless locus in Drosophila. Dev Genet 7 205 221
12. KeyesLN
ClineTW
SchedlP
1992 The primary sex-determination signal of Drosophila acts at the level of transcription. Cell 68 933 943
13. SalzHK
1992 The genetic analysis of snf: A Drosophila sex determination gene required for activation of Sex-lethal in both the germline and the soma. Genetics 130 547 554
14. TaziJ
KornstadtU
RossiF
JeanteurP
CathalaG
1993 Thiophosphorylation of U1-70K protein inhibits pre-mRNA splicing. Nature 363 283 286
15. KotovicKM
LockshonD
BoricL
NeugebauerKM
2003 Cotranscriptional recruitment of the U1 snRNP to intron-containing genes in yeast. Mol Cell Biol 23 5768 5779
16. SwinburneIA
MeyerCA
LiuXS
SilverPA
BrodskyAS
2006 Genomic localization of RNA binding proteins reveals links between pre-mRNA processing and transcription. Genome Res 16 912 921
17. ListermanI
SapraAK
NeugebauerKM
2006 Cotranscriptional coupling of splicing factor recruitment and precursor messenger RNA splicing in mammalian cells. Nat Struct Mol Biol 13 815 822
18. BrodskyAS
MeyerCA
SwinburneIA
HallG
KeenanBJ
2005 Genomic mapping of RNA polymerase II reveals sites of co-transcriptional regulation in human cells. Genome Biol 6 R64
19. WangX
LeeC
GilmourDS
GergenJP
2007 Transcription elongation controls cell fate specification in the Drosophila embryo. Genes Dev 21 1031 1036
20. SamuelsME
BoppD
ColvinRA
RoscignoRF
Garcia-BlancoMA
1994 RNA binding by SXL proteins in vitro and in vivo. Mol Cell Biol 14 4975 4990
21. SosnowskiBA
BeloteJM
McKeownM
1989 Sex–specific alternative splicing of RNA from the transformer gene results from sequence–dependent splice site blockage. Cell 3 449 459
22. BellLR
HorabinJI
SchedlP
ClineTW
1991 Positive autoregulation of Sex-lethal by alternative splicing maintains the female determined state in Drosophila. Cell 65 229 239
23. HeroldN
WillCL
WolfE
KastnerB
UrlaubH
2009 Conservation of the protein composition and electron microscopy structure of Drosophila melanogaster and human spliceosomal complexes. Mol Cell Biol 29 281 301
24. MountSM
SalzHK
2000 Pre-messanger RNA processing factors in the Drosophila melanogaster genome. J Cell Biol 150 37 43
25. PanditS
WangD
FuXD
2008 Functional integration of transcriptional and RNA processing machineries. Curr Opin Cell Biol 20 260 265
26. ShiX
KachirskaiaI
WalterKL
KuoJH
LakeA
2007 Proteome-wide analysis in Saccharomyces cerevisiae identifies several PHD fingers as novel direct and selective binding modules of histone H3 methylated at either lysine 4 or lysine 36. J Biol Chem 282 2450 2455
27. PrietoI
KouznetsovaA
FuttererA
TrachanaV
LeonardoE
2009 Synaptonemal complex assembly and H3K4Me3 demethylation determine DIDO3 localization in meiosis. Chromosoma 118 617 632
28. DoerksT
CopleyRR
SchultzJ
PontingCP
BorkP
2002 Systematic identification of novel protein domain families associated with nuclear functions. Genome Res 12 47 56
29. DaubresseG
DeuringR
MooreL
PapoulasO
ZakrajsekI
1999 The Drosophila kismet gene is related to chromatin-remodeling factors and is required for both segmentation and segment identity. Development 126 1175 1187
30. WindM
ReinesD
2000 Transcription elongation factor SII. Bioessays 22 327 336
31. AriyoshiM
SchwabeJW
2003 A conserved structural motif reveals the essential transcriptional repression function of Spen proteins and their role in developmental signaling. Genes Dev 17 1909 1920
32. Sanchez-PulidoL
RojasAM
van WelyKH
Martinez-AC
ValenciaA
2004 SPOC: a widely distributed domain associated with cancer, apoptosis and transcription. BMC Bioinformatics 5 91
33. AllemandE
BatscheE
MuchardtC
2008 Splicing, transcription, and chromatin: a menage a trois. Curr Opin Genet Dev 18 145 151
34. SimsRJr
MillhouseS
ChenCF
LewisBA
Erdjument-BromageH
2007 Recognition of trimethylated histone H3 lysine 4 facilitates the recruitment of transcription postinitiation factors and pre-mRNA splicing. Mol Cell 28 665 676
35. BatscheE
YanivM
MuchardtC
2006 The human SWI/SNF subunit Brm is a regulator of alternative splicing. Nat Struct Mol Biol 13 22 29
36. FuttererA
CampaneroMR
LeonardoE
CriadoLM
FloresJM
2005 Dido gene expression alterations are implicated in the induction of hematological myeloid neoplasms. J Clin Invest 115 2351 2362
37. MinakhinaS
StewardR
2006 Melanotic mutants in Drosophila: pathways and phenotypes. Genetics 174 253 263
38. GiotL
BaderJS
BrouwerC
ChaudhuriA
KuangB
2003 A protein interaction map of Drosophila melanogaster. Science 302 1727 1736
39. LarochelleS
PandurJ
FisherR
SalzHK
SuterB
1998 Cdk7 is essential for mitosis and for in vivo Cdk-activating kinase activity. Genes Dev 12 370 381
40. MaineEM
SalzHK
ClineTW
SchedlP
1985 The Sex-lethal gene of Drosophila: DNA alterations associated with sex-specific lethal mutations. Cell 43 521 529
41. SalzHK
ClineTW
SchedlP
1987 Functional changes associated with structural alterations induced by mobilization of a P element inserted in the Sex-lethal gene of Drosophila. Genetics 117 221 231
42. CronmillerC
SchedlP
ClineTW
1988 Molecular characterization of daughterless, a Drosophila sex determination gene with multiple roles in development. Genes Dev 2 1666 1676
43. HabetsWJ
HoetMH
de JongBAW
van der KempA
van VenrooijWJ
1989 Mapping of B cell epitopes on small nuclear ribonucleoproteins that react with human autoantibodies as well as with experimentally-induced mouse monoclonal antibodies. J Immunol 143 2560 2566
44. FlickingerTW
SalzHK
1994 The Drosophila sex determination gene snf encodes a nuclear protein with sequence and functional similarity to the mammalian U1A snRNP protein. Genes Dev 8 914 925
45. NagengastAA
SalzHK
2001 The Drosophila U2 snRNP-U2A' protein has an essential function that is SNF/U2B″ independent. Nucl Acids Res 29 3841 3847
46. BoppD
BellLR
ClineTW
SchedlP
1991 Developmental distribution of female-specific Sex-lethal proteins in Drosophila melanogaster. Genes Dev 5 403 415
47. AndrulisED
GuzmanE
DoringP
WernerJ
LisJT
2000 High-resolution localization of Drosophila Spt5 and Spt6 at heat shock genes in vivo: roles in promoter proximal pausing and transcription elongation. Genes Dev 14 2635 2649
48. TieF
StrattonCA
KurzhalsRL
HartePJ
2007 The N terminus of Drosophila ESC binds directly to histone H3 and is required for E(Z)-dependent trimethylation of H3 lysine 27. Mol Cell Biol 27 2014 2026
49. TieF
FuruyamaT
Prasad-SinhaJ
JaneE
HartePJ
2001 The Drosophila Polycomb Group proteins ESC and E(Z) are present in a complex containing the histone-binding protein p55 and the histone deacetylase RPD3. Development 128 275 286
50. StitzingerS
ConradT
ZachlinA
SalzHK
1999 Functional analysis of SNF, the Drosophila U1A/U2B″ homolog: identification of dispensable and indispensable motifs for both snRNP assembly and function. RNA 5 1440 1450
51. Birch-MachinI
GaoS
HuenD
McGirrR
WhiteRA
2005 Genomic analysis of heat-shock factor targets in Drosophila. Genome Biol 6 R63
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
2010 Číslo 3
- Gynekologové a odborníci na reprodukční medicínu se sejdou na prvním virtuálním summitu
- Je „freeze-all“ pro všechny? Odborníci na fertilitu diskutovali na virtuálním summitu
Najčítanejšie v tomto čísle
- Deciphering Normal Blood Gene Expression Variation—The NOWAC Postgenome Study
- Papillorenal Syndrome-Causing Missense Mutations in / Result in Hypomorphic Alleles in Mouse and Human
- Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of Congenital Generalized Lipodystrophy with Muscle Rippling (CGL4) Due to Mutations
- HAP2(GCS1)-Dependent Gamete Fusion Requires a Positively Charged Carboxy-Terminal Domain